Automatic analyzing device

ABSTRACT

A reaction solution is mixed in a short period of time with excellent stir efficiency. A stir rod  19  is vertically reciprocated in a reaction solution  7  during the stirring of the solution.

TECHNICAL FIELD

The present invention relates to an automatic analyzing device, and to an automatic analyzing device including a stir mechanism for mixing a reagent, a reaction solution, and the like which are injected into a container.

BACKGROUND ART

A biochemical automatic analyzing device is known which performs biochemical analysis on a sample, such as blood, urine, or stool, by injecting the sample and a reagent into a transparent measurement container called a sample cell to react them with each other, and then optically measuring the coloration due to the reaction of the reaction solution including the sample and the reagent (refer to Patent Document 1, for example).

In this regard, after both the reagent and the sample are injected into the sample cell, the reagent and the sample are stirred in the sample cell in order to react with each other favorably and uniformly. For a biochemical automatic analyzing device, a stir mechanism which mixes a reaction solution in a short period of time is demanded in terms of improvement in throughput. Further, in terms of reduction in the consumption volume of reagent, there is a demand for a stir mechanism that mixes a reaction solution in a minute sample cell with which a small volume of reaction solution can be analyzed.

Patent Document 2 proposes a method of causing a stir rod to perform a rotational movement and a reciprocal rectilinear movement in a horizontal direction at the same time for efficient stirring in a short period of time. However, analysis has to be performed with a narrow sample cell in order to handle a smaller volume of reaction solution. This requires the stirring to be performed with a limited horizontal movement.

CITATION LIST Patent Document

-   Patent Document 1: U.S. Pat. No. 4,451,433 -   Patent Document 2: JP 10-62430 A

DISCLOSURE OF THE INVENTION Problems to be Solved by the Invention

As for a stir mechanism that involves the rotation of a stir rod, a phenomenon is recognized in which the flow of a solution is vertically separated into multiple layers once the solution reaches its steady state. It has been found out as a result of research that the number of layers formed by separation and the rate of propagation of a substance between the layers affect the uniformity of a stirred reaction solution. Since the rate of propagation of a substance between layers is lower than the rate of propagation of a substance within each layer, the uniformity of a reaction solution decreases with a larger number of layers formed by separation. Further, the number of layers formed by separation tends to increase in a case where a sample cell is narrow, where the volume of reaction solution is large, and where the viscosity of the reaction solution in the sample cell is high. In the field of biochemistry, various volumes of reagents with various properties are used. Accordingly, it is difficult to control the number of layers formed by separation, and is particularly difficult to make a solution uniform by stirring the solution in a short period of time in a minute sample cell suited to a small volume of reaction solution.

Means for Solving the Problems

In order to solve the above problems, according to the present invention, a stir rod is rotated and vertically reciprocated at the same time to efficiently mix a sample and a reagent or a reaction solution to be stirred. By vertically reciprocating a stir rod during a stir operation of rotating the stir rod in a reaction solution, a boundary surface between layers of flow generated in the steady state disappears and the rate of propagation of a substance increases, thus enabling efficient mixing.

Effects of the Invention

In the present invention, performing a rotational movement and a vertical reciprocating movement at the same time scrambles the flow vertically separated into multiple layers in the steady state and thereby enables efficient propagation of a substance between the layers, and thus improvement of the stir efficiency. The present invention is an advantageous means especially for the case of stirring in a minute sample cell in a short period of time.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a diagram showing an example of a configuration of an automatic analyzing device.

FIGS. 2A to 2C are views showing an example of a configuration of a stir unit.

FIGS. 3A to 3C are views showing a conventional stir process.

FIG. 4 is a time chart showing a relation between the height of and the rotation rate of a stir rod in the conventional stir process.

FIGS. 5A to 5C are diagrams showing the number of layers formed by separation during the stirring.

FIGS. 6A to 6E are views showing a stir process including a vertical reciprocating movement according to the present invention.

FIG. 7 is a time chart showing a relation between the height of and the rotation rate of a stir rod in the stir process of the present invention.

FIG. 8 is a diagram showing the nonuniformity of a glycerine solution after the stirring with/without the vertical reciprocating movement.

FIG. 9 is a diagram illustrating a control system for the vertical reciprocating movement according to the present invention.

FIG. 10 is a diagram showing associations between test-request input information and stir conditions.

MODES FOR CARRYING OUT THE INVENTION

Embodiments of the present invention will be described in detail below with reference to the drawings.

First Embodiment

FIG. 1 shows an example of an overall configuration of an automatic analyzing device according to the present invention. Multiple sample cups 2 each housing therein a sample 1 are arranged in a sample disk 3. Multiple reagent cups 5 each housing therein a reagent 4 are arranged in a reagent disk 6. Multiple sample cells 8 are arranged in a cell disk 9. Each sample cell 8 is used to mix the sample 1 with the reagent 4 to make a reaction solution 7. A sample pipetting mechanism 10 is capable of moving a predetermined volume of sample 1 from the inside of one of the sample cups 2 to the inside of one of the sample cells 8. A reagent pipetting mechanism 11 is capable of moving a predetermined volume of reagent 4 from the inside of one of the reagent cups 5 to the inside of one of the sample cells 8. A stir unit 12, a measurement unit 13, and a cleaning unit 14 are arranged around the cell disk 9. The stir unit 12 stirs and mixes the sample 1 with the reagent 4 in each sample cell 8. The measurement unit 13 performs optical measurement on the reaction solutions. The cleaning unit 14 cleans the sample cells 8. The measurement unit 13 includes a light source 15 and a light receiving element 18. The light source 15 irradiates the reaction solution 7 with light. The light receiving element 8 receives light obtained by the irradiation of the reaction solution 7 with light. The sample cells 8 arranged in the cell disk 9 and the reaction solutions 7 in the cells are kept at a predetermined temperature by an constant temperature fluid 17 held in a thermostatic chamber. The automatic analyzing device also includes: a control part which controls parts of the device; a data storage part which stores therein various data; an input part through which required data can be inputted from the outside; a measurement part which calculates the absorbance of light from the amount of light received at the light receiving element 18; an analysis part which finds the amounts of ingredients from the absorbance; and an output part which is capable of displaying data and outputting the data to the outside.

The analysis of the amount of a certain ingredient in the sample 1 is conducted with the following procedure. First, the sample pipetting mechanism 10 pipettes a predetermined volume of sample 1 contained in one of the sample cups 2 into one of the sample cells 8. Next, the reagent pipetting mechanism 11 pipettes a predetermined volume of reagent 4 contained in one of the reagent cups 5 into the sample cup 2. Subsequently, the stir unit 12 stirs the sample 1 and the reagent 4 in the sample cell 8 to make the reaction solution 7. If necessary, the reagent pipetting mechanism 11 additionally pipettes multiple reagents 4 into the sample cell 8. In the pipetting, the sample disk 3, the reagent disk 6, and the cell disk 9 are rotated to move the sample cup 2, the reagent cup 5, and the sample cell 8 to predetermined positions, respectively. After the reaction, the cleaning unit 14 cleans the inside of the sample cell 8 for next analysis. The measurement unit 13 and the measurement part measure the absorbance of the reaction solution 7, and the absorbance data is stored in the data storage part. The analysis part is capable of analyzing the amount of the ingredient from the stored absorbance data on the basis of calibration curve data and the Lambert-Beer law. Data required for the control on each part and the analysis is inputted into the data storage part through the input part. The various data and analysis result are displayed and outputted by the output part.

FIG. 2A shows an example of a configuration of the stir unit 12. The stir unit 12 of this example includes: a stir rod 19; a rotation motor 21 which is coupled to the stir rod 19 through gears 20 a, 20 b, and 20 c; a first support member 22 which supports the rotation motor 21; a horizontal movement motor 23 which is coupled to the first support member; a second support member 24 which supports the horizontal movement motor 23; and a vertical motor 26 which is coupled to the second support member 24 through a crank 25. Further, general shapes of the stir rod 19 include a flat-plate shape as shown as an enlarged view in FIG. 2B and a screw shape as shown as an enlarged view in FIG. 2C. The present invention is advantageous for the stir rod of any of these shapes.

To clarify a difference between a stir process according to the present invention and a conventional stir process, the conventional stir process will be described first. The stir unit 12 conventionally stirs a reaction solution 7 with the following procedure. First, the horizontal movement motor 23 is driven to move the stir rod 19 to a position above one of the sample cells 8. Next, the vertical motor 26 is driven to insert the stir rod 19 into the reaction solution 7 in the sample cell 8. Subsequently, the rotation motor 21 is driven to rotate the stir rod 19 in the reaction solution 7, thereby performing the stir operation. Thereafter, the vertical motor 26 is driven to pull out the stir rod 19 to the position above the sample cell 8. The procedure described above is the process of stirring the reaction solution 7 by the stir unit 12, and a process of cleaning the stir rod 19 continues after this process. In the process of cleaning the stir rod, the horizontal movement motor 23 is driven to move the stir rod 19 to a position above a cleaning tank in the cleaning unit 14. Next, the vertical motor 26 is driven to insert the stir rod 19 into the cleaning tank. Subsequently, the rotation motor 21 is driven to rotate the stir rod 19 inside the cleaning tank, thereby performing the cleaning operation. Thereafter, the vertical motor 26 is driven to pull out the stir rod 19 to the position above the cleaning tank.

FIGS. 3A to 3C are schematic views showing a conventional stir process. FIG. 4 is a time chart showing a relation between the height of a bottom end of the stir rod 19 and the rotation rate thereof in the conventional stir process. FIG. 3A shows the step of causing the vertical motor 26 to insert the stir rod 19 into the reaction solution 7 in the sample cell 8. This process corresponds to time t₀ to time t₁ in FIG. 4. The stir rod 19 descends from a height h₀ to a height h₁, and accelerates its rotation rate from r₀ of a stopped state to r₁. h₂ indicates the height of the reaction solution 7 and varies depending on the volume of the solution. FIG. 3B shows the step of causing the rotation motor 21 to rotate the stir rod 19 in the reaction solution 7 to stir the solution. This process corresponds to the time t₁ to time t₂ in FIG. 4. The stir rod 19 is kept at a height of h₁ and at a rotation rate of r₁. FIG. 3C shows the step of pulling out the stir rod 19 to a position above the sample cell 8. This process corresponds to the time t₂ to time t₃ in FIG. 4. The stir rod 19 ascends from the height h₁ to the height h₀, and decelerates its rotation rate from r₁ to r₀ to stop.

Here, if the stir rod 19 inserted into or pulled out from the reaction solution 7 while rotating at a high speed during the time t₀ to the time t₁ or during the time t₂ to the time t₃, the reaction solution 7 may splash on the surface of the solution and attach to a wall surface of the sample cell 8, thus affecting the analysis accuracy in some cases. Accordingly, in order to avoid the splash of the reaction solution 7, the conventional stir process causes the stir rod 19 to perform a vertical movement with its rotation being completely stopped or with a low rotation rate by adjusting the rotation rate when the stir rod 19 passes the position of the height h₂, and to perform a rotational movement at a fixed position of the height h₁ during the time t₁ to t₂ after it is inserted and before it is pulled out. If the stir rod 19 performs the rotational movement at the fixed position, the solution reaches its steady state, and a boundary surface of flow 27 is generated in the reaction solution 7 as shown in FIG. 3B. FIG. 3B shows an example where one boundary surface of flow 27 is generated. If the boundary surface of flow 27 is generated, the reaction solution 7 in the sample cell 8 is separated vertically at the boundary surface of flow 27, and independent flows are generated in the upper side and the lower side of the reaction solution, respectively.

FIGS. 5A and 5B show the number of layers formed by the separation during the stirring. FIG. 5C shows a cubic diagram of the sample cell 8. In FIG. 5C, the width indicates a dimension orthogonal to a traveling direction of light for measurement 16, the length indicates a dimension parallel to the traveling direction of the light for measurement 16, and the height indicates the height of the reaction solution 7. 0% to 40% glycerine was pipetted into each of two kinds of sample cells A (width: 2.5 mm, length: 5.0 mm) and B (width: 2.5 mm, length: 3.0 mm), the resultant solution in each cell was stirred by a screw-shaped stir rod of 1.5 mm width, and the separation of the flow was observed. As a result, it was found out that the number of layers formed by the separation was two or more under any condition. In particular, the tendency of increase in the number of layers to three or more is significantly observed under the conditions where the aspect ratio of the height of the reaction solution 7 to the 2.5 mm width is 3:1 or higher. In this event, the rate of propagation of a substance in the sample 1 or the reagent 4 is lower between layers separated by the boundary surface of flow 27, than within each layer. Hence, the larger the number of boundary surfaces of flow 27, the lower the uniformity of the sample 1 and the reagent 4 in the reaction solution 7 after the stirring.

Next, a stir process including a vertical reciprocating movement according to the first embodiment of the present invention is shown in FIGS. 6A to 6E. FIG. 7 is a time chart showing a relation between the height of the bottom end of the stir rod 19 and the rotation rate thereof in the stir process of the present invention.

FIG. 6A shows a step of causing the vertical motor 26 to insert the stir rod 19 into the reaction solution 7 in one of the sample cells 8. This process corresponds to time t₀ to time t₁ in FIG. 7. The stir rod 19 descends from a height h₀ to a height h₁, and accelerates its rotation rate from r₀ of a stopped state to r₁. h₂ indicates the height of the reaction solution 7. FIG. 6B shows a step of causing the rotation motor 21 to rotate the stir rod 19 at a fixed position in the reaction solution 7 to stir the solution. This process corresponds to the time t₁ to time t₄ in FIG. 7. The stir rod 19 is kept at a height of h₁ and at a rotation rate of r₁ at which the rod achieves high-speed stable rotation. FIGS. 6C and 6D show steps of causing the vertical motor 26 to vertically reciprocate the stir rod 29 in such a manner as to move the stir rod upward from the fixed position h₁ once and downward to the fixed position again in the reaction solution 7, while causing the rotation motor 21 to rotate the stir rod. The process shown in FIGS. 6C and 6D corresponds to the time t₄ to time t₅ in FIG. 7. The stir rod 19 is vertically reciprocated between the height h₁ and a height h₃ with the rotation rate being kept at r₁. FIG. 6E shows a step of pulling out the stir rod 19 to a position above the sample cell 8. This process corresponds to time t₂ to time t₃ in FIG. 7. The stir rod 19 ascends from the height h₁ to the height h₀, and decelerates its rotation rate from r₁ to r₀ to stop.

Here, in FIG. 6B, a boundary surface of flow 27 is generated in the reaction solution 7 when the solution reaches its steady state. However, by rotating and vertically reciprocating the stir rod 19 at the same time as shown in FIGS. 6C and 6D, a layer of turbulent flow 28 is formed around the area where the boundary surface of flow 27 has been generated. This increases the rate of propagation of a substance in the sample 1 or the reagent 4 between layers separated by the boundary surface of flow 27, and thus increases the uniformity of the sample 1 and the reagent 4 in the reaction solution 7 after the stirring. In this event, since the stir rod 19 is vertically reciprocated in a state where the stir rod 19 is immersed in the reaction solution 7, no reaction solution 7 splashes even when the stir rod 19 rotates at a high speed.

FIG. 8 shows a result of evaluating the nonuniformity of a glycerine solution after the stirring with/without the vertical reciprocating movement by using a simple evaluation device. A total of 130 μL of a pigment solution and a glycerine solution was pipetted into a sample cell 8 of 2.5 mm width and 5.0 mm length, and the resultant solution was stirred by a screw-shaped stir rod 19 of 1.5 mm width. Under the condition with the vertical reciprocating movement, the stir rod 19 in high-speed stable rotation was vertically reciprocated in such a manner that the tip of the stir rod 19 was moved once between a position 1.0 mm above the bottom surface of the sample cell 8 and a position 2.0 mm thereabove. Under the condition without the vertical reciprocating movement, the stirring was performed under the same condition except that the tip of the stir rod was kept at the position 1.0 mm above the bottom surface of the sample cell 8. Variation in the concentration of the solution was found from the brightness of an image obtained by photographing of the stirred solution, and thereby the nonuniformity of the solution was calculated.

As a result, as shown in FIG. 8, the uniformity of the solution with a glycerine concentration in a range of 0% to 40% was higher under the condition with the vertical reciprocating movement than under the condition without the vertical reciprocating movement. The result of FIG. 8 shows that the vertical reciprocating movement is effective in the case of using a container of 2.5 mm width. Further, the present invention is advantageous in the case of using a container of 2.5 mm dimension or smaller since the separation into layers is more likely to occur in a container of smaller dimension. Although the vertical reciprocating movement was performed in the range of 1.0 mm to 2.0 mm above the bottom surface of the sample cell 8 in this embodiment, any moving range of the vertical reciprocating movement can be set as long as the stir rod 19 is so reliably immersed in the reaction solution 7 that no splash occurs, and does not come into contact with the bottom surface of the sample cell 8 in this range.

Second Embodiment

FIG. 9 shows a control flow of the vertical reciprocating movement according to a second embodiment of the present invention. A requested test item and an analysis condition are inputted through the input part, and are stored in a setting part of analysis condition 30 in a storage 29. The setting part of analysis condition 30 inquires of a memory part of analysis parameter 31 about analysis parameters as needed. Next, the setting part of analysis condition 30 transmits the analysis condition to an automatic setting part of stir condition 32. Then, the automatic setting part of stir condition 32 reads, from a memory part of stir parameter 33, a stir condition associated with the volume of a reaction solution and the type of a reagent included in the analysis condition, and automatically sets parameters such as on/off of the stirring reciprocating movement and a vertical movement distance.

FIG. 10 is a diagram showing an example of associations between test-request input information and stir conditions. It is possible to previously store a database in the memory part of stir parameter 33 and determine stir conditions on the basis of input information from the input part. As shown in FIG. 10, the database associates input information, such as a test item and the volume of a sample or a reagent, with the type of reagent and stir conditions such as on/off of the vertical reciprocating movement and a reciprocating movement distance. This allows an automatic setting of stir conditions without an input of the stir conditions by the user. Thereafter, the setting part of analysis condition 30 transmits the analysis parameters to a control part of sample pipetting unit 34 and a control part of reagent pipetting unit 35, and the automatic setting part of stir condition 32 transmits the stir condition parameters to a control part of stir unit 36. The unit control parts thereby drive the sample pipetting unit 10, the reagent pipetting unit 11, and the stir unit 12, respectively.

REFERENCE SIGN LIST

-   1 sample -   2 sample cup -   3 sample disk -   4 reagent -   5 reagent cup -   6 reagent disk -   7 reaction solution -   8 sample cell -   9 cell disk -   10 sample pipetting mechanism -   11 reagent pipetting mechanism -   12 stir unit -   13 measurement unit -   14 cleaning unit -   15 light source -   16 light -   17 constant temperature fluid -   18 light receiving element -   19 stir rod -   20 a to 20 c gear -   21 rotation motor -   22 first support member -   23 horizontal movement motor -   24 second support member -   25 crank -   26 vertical motor -   27 boundary surface of flow -   28 layer of turbulent flow -   29 storage -   30 setting part of analysis condition -   31 memory part of analysis parameter -   32 automatic setting part of stir condition -   33 memory part of stir parameter -   34 control part of sample pipetting unit -   35 control part of reagent pipetting unit -   36 control part of stir unit 

1. An automatic analyzing device characterized by comprising: a sample cell; a sample cell conveying part configured to convey the sample cell; a sample injecting part configured to inject a sample into the sample cell; a reagent injecting part configured to inject a reagent into the sample cell; a stir part configured to stir a solution in the sample cell; a measurement part configured to perform optical measurement on the solution in the sample cell by irradiating the solution with light; and a control part configured to control each part, characterized in that the stir part includes: a stir rod to be inserted into the solution in the sample cell; a rotation motor configured to drive the stir rod to rotate; and a vertical motor configured to move the stir rod up and down, and the control part drives the rotation motor to rotate the stir rod and drives the vertical motor to vertically reciprocate the stir rod in the solution in the sample cell at the same time to stir the solution in the sample cell.
 2. The automatic analyzing device according to claim 1, characterized in that at least one of a width and a length of the sample cell is 2.5 mm or smaller.
 3. The automatic analyzing device according to claim 1, characterized in that the control part drives the vertical motor to vertically reciprocate the stir rod in such a manner as to drive the stir rod to move upward from a fixed position once and to go back to the fixed position in the solution in the sample cell, during a stir operation in which the stir rod inserted in the solution in the sample cell is rotationally driven at the fixed position by the rotation motor.
 4. The automatic analyzing device according to claim 1, characterized in that the control part causes the vertical motor to move the stir rod downward to put the stir rod into the solution in the sample cell while the rotation motor is stopped or accelerated, drives the vertical motor to vertically reciprocate the stir rod while the rotation rod is rotating at a high-speed after the rotation rod moves to the fixed position and the rotation motor finishes the acceleration, and thereafter causes the vertical motor to move the stir rod upward to pull the stir rod out of the solution in the sample cell while the rotation motor is stopped or decelerated.
 5. The automatic analyzing device according to claim 1, characterized by further comprising: an input part configured to receive an input of data on a test item and an analysis condition; and a memory part of stir parameter configured to store therein a correlation between a stir condition and a volume of the solution in the sample cell or a type of the reagent, characterized in that the control part sets whether or not the vertical motor should vertically reciprocate the stir rod or sets a distance of the vertical reciprocating movement by checking the data inputted through the input part against the correlation stored in the memory part of stir parameter. 